ENST00000471862.2:n.2602G>A
(COL4A3)
|
|
|
ENST00000682257.1:n.566G>A
(COL4A3)
|
|
|
ENST00000682970.1:n.642G>A
(COL4A3)
|
|
|
ENST00000683077.1:n.2283G>A
(COL4A3)
|
|
|
ENST00000684413.1:n.2911G>A
(COL4A3)
|
|
|
ENST00000684724.1:n.765G>A
(COL4A3)
|
|
|
ENST00000396578.8:c.*331G>A
(COL4A3)
MANE Select
|
ENSP00000379823.3:n.*331G>A
|
|
ENST00000396578.7:c.*331G>A
(COL4A3)
|
ENSP00000379823.3:n.*331G>A
|
|
NM_000091.4:c.*331G>A , LRG_230t1:c.*331G>A
(COL4A3)
|
NP_000082.2:n.*331G>A
|
|
NR_102371.1:n.48-6546C>T
(MFF-DT)
|
|
|
XM_005246276.2:c.*257G>A
(COL4A3)
|
XP_005246333.1:n.*257G>A
|
|
XM_005246277.2:c.*331G>A
(COL4A3)
|
XP_005246334.1:n.*331G>A
|
|
XM_011510556.1:c.*331G>A
(COL4A3)
|
XP_011508858.1:n.*331G>A
|
|
XR_241280.2:n.5304G>A
(COL4A3)
|
|
|
XM_005246277.3:c.*331G>A
(COL4A3)
|
XP_005246334.1:n.*331G>A
|
|
XM_011510556.2:c.*331G>A
(COL4A3)
|
XP_011508858.1:n.*331G>A
|
|
XR_241280.3:n.5304G>A
(COL4A3)
|
|
|
NM_000091.5:c.*331G>A
(COL4A3)
MANE Select
|
NP_000082.2:n.*331G>A
|
|